Evidence map›Paper›PMID 35319248›Full record

ArticleMicrobiology spectrum2022

Multiple Routes of Antibody-Dependent Enhancement of SARS-CoV-2 Infection.

Kosuke Okuya, Takanari Hattori, Takeshi Saito, Yoshihiro Takadate, Michihito Sasaki, Wakako Furuyama, Andrea Marzi, Yoichi Ohiro, Satoshi Konno, Takeshi Hattori and 1 more

Open access · goldAbstract read
In one paragraph

Article in Microbiology spectrum, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 1 pooled it
5.1field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

41 citing papers in PubMed, 1 synthesis or guideline pooled it, 50 citations in OpenAlex.

  1. Pooled it
  2. Review
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  6. Article
  7. Article
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  9. Article
  10. Antibody-dependent enhancement of coronaviruses.International journal of biological sciences · 2025
    Review
  11. Article
  12. Article
  13. Strategies of rational and structure-driven vaccine design for Arenaviruses.Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases · 2024
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 2 countries.

Kosuke OkuyaDivision of Global Epidemiology, International Institute for Zoonosis Control, Hokkaido Universitygrid.39158.36grid.412167.7, Sapporo, Japan.ORCID 0000-0002-7987-9884
Takanari HattoriDivision of Global Epidemiology, International Institute for Zoonosis Control, Hokkaido Universitygrid.39158.36grid.412167.7, Sapporo, Japan.
Takeshi SaitoDivision of Global Epidemiology, International Institute for Zoonosis Control, Hokkaido Universitygrid.39158.36grid.412167.7, Sapporo, Japan.
Yoshihiro TakadateDivision of Global Epidemiology, International Institute for Zoonosis Control, Hokkaido Universitygrid.39158.36grid.412167.7, Sapporo, Japan.
Michihito SasakiDivision of Molecular Pathobiology, International Institute for Zoonosis Control, Hokkaido Universitygrid.39158.36grid.412167.7, Sapporo, Japan.ORCID 0000-0003-1607-2175
Wakako FuruyamaLaboratory of Virology, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rocky Mountain Laboratories, Hamilton, Montana, USA.
Andrea MarziLaboratory of Virology, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rocky Mountain Laboratories, Hamilton, Montana, USA.ORCID 0000-0003-0186-9587
Yoichi OhiroDepartment of Oral and Maxillofacial Surgery, Hokkaido Universitygrid.39158.36grid.412167.7 Graduate School of Dental Medicine, Sapporo, Japan.
Satoshi KonnoDepartment of Respiratory Medicine, Faculty of Medicine and Graduate School of Medicine, Hokkaido Universitygrid.39158.36grid.412167.7, Sapporo, Japan.
Takeshi HattoriDepartment of Respiratory Medicine, National Hospital Organization Hokkaido Medical Center, Sapporo, Japan.
Ayato TakadaDivision of Global Epidemiology, International Institute for Zoonosis Control, Hokkaido Universitygrid.39158.36grid.412167.7, Sapporo, Japan.ORCID 0000-0003-2464-6642
Hokkaido University · JPNational Institutes of Health · US

Funding

Countermeasures against COVID-19ZIAAI001284 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI MARZI, ANDREA · 2020 to 2023
$403k
6 · The paper itself

Abstract

Antibody-dependent enhancement (ADE) of infection is generally known for many viruses. A potential risk of ADE in severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection has also been discussed since the beginning of the coronavirus disease 2019 (COVID-19) pandemic; however, clinical evidence of the presence of antibodies with ADE potential is limited. Here, we show that ADE antibodies are produced by SARS-CoV-2 infection and the ADE process can be mediated by at least two different host factors, Fcγ receptor (FcγR) and complement component C1q. Of 89 serum samples collected from acute or convalescent COVID-19 patients, 62.9% were found to be positive for SARS-CoV-2-specific IgG. FcγR- and/or C1q-mediated ADE were detected in 50% of the IgG-positive sera, whereas most of them showed neutralizing activity in the absence of FcγR and C1q. Importantly, ADE antibodies were found in 41.4% of the acute COVID-19 patients. Neutralizing activity was also detected in most of the IgG-positive sera, but it was counteracted by ADE in subneutralizing conditions in the presence of FcγR or C1q. Although the clinical importance of ADE needs to be further investigated with larger numbers of COVID-19 patient samples, our data suggest that SARS-CoV-2 utilizes multiple mechanisms of ADE. C1q-mediated ADE may particularly have a clinical impact since C1q is present at high concentrations in plasma and its receptors are ubiquitously expressed on the surfaces of many types of cells, including respiratory epithelial cells, which SARS-CoV-2 primarily infects.

Indexed as

Antibody-Dependent EnhancementCOVID-19Antibodies, NeutralizingAntibodies, ViralComplement C1qHumansImmunoglobulin GReceptors, IgGSARS-CoV-2Antibodies, NeutralizingAntibodies, ViralComplement C1qImmunoglobulin GReceptors, IgGADEantibody-dependent enhancementC1qcomplementCOVID-19FcRFc receptorSARS-CoV-2

Identifiers

PMID35319248
PMCPMC9045191
OpenAlexW4220886005

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.